Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
  • C09B1/16—Amino-anthraquinones
  • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
  • C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
  • C09B1/16—Amino-anthraquinones
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
  • C09B1/56—Mercapto-anthraquinones
  • C09B1/58—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals
  • C09B1/60—Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals substituted by aliphatic, cycloaliphatic or araliphatic radicals

Definitions

• R is an optionally substituted phenyl radical; and Y is H, Cl, Br or S-X--OH have been prepared.
• the subject-matter of the present invention comprises dyestuffs of the general formula stituted by a hydroxyl group; R and R, stand for optionally substituted alkyl or cycloalkyl radicals; and Y stands for hydrogen, chlorine, bromine or SXOl-l where X has the same meaning as above and the anthraquinone nucleus may contain further substituents, preferably halogen,
• X stands for an alkylene radical whichmay be substituted by a hydroxyl group
• R and R stand for hydrogen or a substituent
• n and m mean the numbers 3
• Y stands for hydrogen, chlorine, bromine or the radical SX-OH where X has the same meaning as above and the anthraquinone nucleus may contain further substituents, especially chlorine or bromine,
• Suitable radicals X are primarily straight-chain or branched alkylene radicals with one to six carbon atoms, for example, ethylene, propylene, Z-hydroxy-propylene and isobutylene radicalsv
• alkyl radicals R and R are primarily alkyl radicals with one to eight carbon atoms, which may be substituted, such as methyl, ethyl, n-, iso-propyl, n-, iso-,tert.-butyl, n-, isopentyl, Z-hydroxy-ethyl, 3-methoxypropyl, benzyl, phenyl-a or -,6-ethyl, l phenyl--methyl-hexylene-( 3 hexahydrobenzyl, y-dimethyl-amino-propylenamino, fl-aminoethyl, 'y-arninopropyl, B-acetaminoeth
• the cycloalkyl radicals are preferably cyclohexyl radicals which may contain one or more of the substituents'customary in anthraquinone chemistry, such as optionally substituted alkyl radicals, preferably those with one to four carbon atoms. for example, methyl, ethyl, n-, iso-propyl, n-, iso-or tert.-butyl radicals; optionally alkylated hydroxyl or amino groups, such as the hydroxyl, methoxy, amino, or acetylamino group.
• radicals R and R, or R and R may be identical or different.
• Suitable substituents R and R are those customary in anthraquinone chemistry, such as alkyl radicals, preferably lower alkyl radicals with one to six carbon atoms, such as methyl, ethyl, n isoand tert.-butyl, n-, iso-pentyl, hydroxyethyl radicals; alkoxy radicals, preferably alkoxy radicals with one to four carbon atoms, which may be substituted, such as methoxy, ethoxy, propoxy, 2-hydroxyethoxy, 3-hydroxypropoxy, 2-methoxy-ethoxy radicals; alkylmercapto radicals, preferably those with one to four carbon atoms such as methylmercapto, ethylmercapto-radicals; halogen atoms such as fluorine, chlorine or bromine; amino groups which may in turn be substituted by alkyl, acyl or cycloalkyl radicals such as amino, methylamino, dimethyl
• Suitable dyestuffs are, for example, those of the formula zlu Y, 0 NHQ Y2 (l i fi i l in which Y, and Y stand for hydrogen, chlorine, bromine or SX--OH but cannot simultaneously denote hydrogen, chlorine or bromine, 1 as well as those of the formula i R 2)n my f) in which Y, and Y as well as R R n and m have the same meaning as above.
• dyestuffs (1) are the anthraquinones mentioned in the following, which are substituted in the 6- or 7-position, or in the 6,7-position by B- hydroxyethyl-thio, ,B'ydihydroxypropyl-thio, 'y-hydroxypropyl-thio, a-methyl-y-hydroxypropyl-thio groups, or in the 6(7)-position by one of the aforesaid hydroxyalkyl thio groups and in the 7(6)-position by chlorine or bromine: l,4-dicyclohexylamino-, l,4-di-o-, m-, p-methyl-cyclohexyl-amino-, 1,4-di-ethyl-cyclohexylamino-, l,4-di-n-, iso-propyl-cyclohexylamino, l,4-di-p-tert.-butyl-
• dyestuffs (ll) are anthraquinones which are substituted in the 5-01 6position or in the 5,8- or 6,7-position by B-hydroxy-etl'iyl-thio, 3,7- dihydroxypropyl-thio, 'y-hydroxypropyl-thio, a-methyl-'yhydroxypropyl-thio groups, or in the 5(8) or 6(7)-position by a B-hydroxyethyl-thio, B, 'y-hydroxypropyl-thio, -y-hydroxypropyl-thio, a-methyl-y-hydroxypropyl-thio group and in the 8(5)- or 7(6) -position by chlorine or bromine, such as l,4-di- 0-, m-, p-anisidino-; l,4-di-o-, m-, p-toluidino-; l,4-di-anilin0-; l,4di-o-,
• Dyestuffs of the general formula (I) can be obtained from compounds of the general formula 0 I ⁇
• Suitable thinls are, for example O-II CH
• the halogen exchange is preferably carried out in an organic solvent, for example, in methanol, ethanol, butanol, isopropanol, N-methyl-pyrrolidone, e-caprolactam, pyridine, chlorobenzenes, glycol ethers, but preferably in dimethyl formamide.
• the reaction can be carried out at room temperature as well as at an elevated temperature, for example, at temperatures of 200 C, preferably at 60 130 C.
• acid-binding agents for example, in the presence of alkali metal carbonates, alkali metal alcoholates, alkali metal hydroxides, and/or tertiary amines, for example, triethylamine, triethanolamine or N-methyl-N,N- diethanolamine.
• the products obtained by the exchange of halogen may be subsequently halogenated, for example, with chlorine or bromine or with the usual halogenating agents.
• the compounds of the general formula (V) can be obtained either by the exchange of the a-positioned halogen atoms in compounds of the general formula (VI) or by the exchange of the hydroxyl groups in compounds of the general formula r r 1? F H QA z Zzi H I Y H 0 X 4) OH (Vl) (VII) in which 2, and Z, have the same meaning as above, and X, and X stand for chlorine or bromine, for optionally substituted alkylor cycloalkyl-am'ino radicals of the type mentioned above and, if desired, by subsequent oxidation of the leuco reaction products primarily formed from (VII).
• the reactions are generally carried out at an elevated temperature, for example, at 200 C. when starting from (VI), at 50 C when starting from (VII), and optionally in the presence of an acid-binding agent, such as an alkali metal carbonate or acetate.
• an acid-binding agent such as an alkali metal carbonate or acetate.
• the reactions are preferably carried out in organic solvents, for example, in methanol, ethanol, isopropanol, butanol, isobutanol, glycol monomethyl ether, or in an excess of the reacting alkylor cycloalkylamines, or in mixtures of these solvents with water, preferably in the presence of boric acid when starting from (VII), and in butanol, glycol or diglycol ethers, dimethyl formamide, chlorobenzenes, nitrobenzene of in an excess of the reacted amines when starting from (VI).
• organic solvents for example, in methanol, ethanol, isopropanol, butanol, isobutanol, glycol monomethyl ether, or in an excess of the reacting alkylor cycloalkylamines, or in mixtures of these solvents with water, preferably in the presence of boric acid when starting from (VII), and in butanol, glycol or diglycol ethers,
• the compounds (VII) can be prepared from the corresponding quinizarines by reduction according to processes known from the literature.
• Suitable reducing agents are for example, sodium dithionite, zinc dust/hydrochloric acid, aluminum powder/sulphuric acid, ironlglacial acetic acid, or the leuco compound of the anthraquinone derivatives used.
• a variant of the process described above consists in that initially the substituents Z and/or 2 in compounds of the formu la exchanged for the radicals I-IO-X--S; the reaction product of the formula 3 R H OX- S I (l OH (IX) in which Y, stands for hydrogen, halogen or is then reduced to form the corresponding leuco compound; the hydroxyl groups are then simultaneously or successively exchanged for identical or different alkyiand/or cyclo-alkyl amino radicals; and, if desired, the leuco reaction products are oxidized by methods known from the literature to form the corresponding anthraquinone derivatives. in general, however, this procedure offers no advantage over the processes described above.
• the dyestuffs of the formula (ll) can be obtained from compounds of the general formula 5 in which Z stands for chlorine or bromine; p for the numbers l or 2; and R R n and m have the same meaning as above, by exchanging the substituent Z for the radical S- X-OH by the reaction with thiols HS-X-OH, one or two substituents being exchangeable, and optionally by subsequent chlorination or bromination.
• the use of different thiols leads to final dyestuffs with different radicals S-X OH.
• the exchange of Z for S-XOH is preferably carried out in an organic solvent, for example in methanol, ethanol, butanol, isopropanol, N-methyl-pyrrolidone, e-caprolactam, pyridine, chlorobenzene, o-dichlorobenzene of glycol monomethyl ether, but preferably in dimethyl formamide.
• the reaction can be carried out at room temperature as well as at an elevated temperature, for example, at temperatures in the range from 20to 200 C, preferably 60 130 C.
• acid-binding agents for example, in the presence of alkali metal carbonates, alkali metal alcoholates, alkali metal hydroxides, and/or tertiary amines, for example, triethylamine, triethylamine or N-methyl-N,N- diethanolamine.
• the resultant products may be subsequently halogenated, for example, with chlorine or bromine or with the usual halogen-yielding agents.
• the compounds of the formula (X) in which the substituent or substituents Z stand in the B-position can be obtained by the exchange of the a-positioned halogen atoms in compounds of the general formula 14 (Xgll in which R R n and m have the same meaning as above. It is possible initially to exchange only one of the a-positioned halogen atoms for an arylamine radical.
• the intermediate product so prepared which still contains a halogen atom in the a-position, is isolated and reacted in a second operation with another arylamine' then there are obtained diarylamino-anthraquinone derivatives which carry different substituents in the 1,4-position.
• the reactions are generally carried out at an elevated temperature, for example, at 220 C, and generally in the presence of an acid-binding agent, such as an alkali metal carbonate or acetate, optionally with the addition of catalytic amounts of copper or its salts.
• an acid-binding agent such as an alkali metal carbonate or acetate
• Suitable solvents a re for example, butanol, glycol and diglycol ethers, dimethyl formamide, chlorobenzenes, nitrobenzene or, preferably, an excess of the reacting amines.
• Suitable reducing agents for the preparation of the leuco compounds are, for example, sodium dithionite, zinc dust/hydrochloric acid, aluminum/sulphuric acid, iron/acetic acid, or the leuco compound of the anthraquinone derivative used.
• the reaction is preferably carried out in organic solvents, for example, in methanol, ethanol, isopropanol, butanol, isobutanol, glycol monomethyl ether or in an excess of the reacting arylamine, or in mixtures of these solvents with water, preferably in the presence of boric acid,
• organic solvents for example, in methanol, ethanol, isopropanol, butanol, isobutanol, glycol monomethyl ether or in an excess of the reacting arylamine, or in mixtures of these solvents with water, preferably in the presence of boric acid,
• the reaction proceeds already at room temperature and is preferably carried out at an elevated temperature, for example, at 60 C.
• the new dyestuffs are finely divided in the usual way, for example, by pasting with sulphuric acid or an organic solvent. They are suitable for dyeing and printing synthetic fiber materials, especially those of synthetic polyamides, for example, those of poly-e-caprolactam or of condensation products from hexamethylenediamine and adipic acid.
• the greenish blue to blue dyeings obtained are generally characterized by great clarity and good general fastness properties, particularly by good fastness to light and washing.
• EXAMPLE 1 a 100 parts l,4-dicyclohexylamino-6-chloro-anthraquinone are suspended in 100 parts dimethyl formamide at 1 15 120 and mixed with 30 minutes with a solution of 25,2 parts thioglycol and 18.4 parts potassium hydroxide in 25.2 parts methanol. The reaction mixture is stirred at l 10 for 20 minutes, poured onto 1,000 parts of ice water, some concentrated hydrochloric acid is added to improve the filtering property, the product is filtered off with suction, washed neutral, and dried. 109 Parts 1,4-di-cyclohexyla.mino-dhydroxyethylmercapto-anthraquninone of good quality are obtained.
• EXAMPLE 3 a 50 parts l,4-di-n-propylamino-6,7-dichloro-anthraquinone are dissolved in 250 parts dimethyl formamide and mixed within 10 minutes at 100 105 with a solution of 13 parts thioglycol and 9.4 parts potassium hydroxide in 13 parts by volume of methanol, and the reaction mixture is further stirred at the same temperature for l0 minutes. The mixture is diluted with 500 parts methanol, stirred for several hours while cooling with ice, the product is filtered off with suction ans successively washed with methanol and water. 41 parts I ,4-di-n-propylamine-6-hydroxyethylmercapto-7-chloroanthraquinone are obtained.
• leuco-6,7-dichloro-quinizarine obtainable, for example, by treating 6,7-dichloro-quinizarine with aluminum powder in concentrated sulphuric acid at 50 55
• 300 parts n-propylamine, 1,000 parts by volume of ethanol and a solution of 10 parts of boric acid in 50 parts of water are boiled under reflux and with access of air for 5 hours.
• the reaction product which is precipitated when the mixture is stirred cold, if filtered off with suction when cold, washed with ethanol and water, and dried. 72 Parts are obtained.
• EXAMPLE 4 a 70 Parts I ,4-di-cyclohexylamino-6,7-dichloroanthraquinone are stirred in 300 parts dimethyl formamide and mixed at I l0 within 20 minutes with a solution of 16.5 parts thioglycol and 12 parts potassium hydroxide in 16.5 parts methanol. Stirring is continued at the same temperature for 30 minutes. The reaction mixture is diluted with 300 parts by volume of methanol, stirred cold, the precipitated reaction product is filtered off with suction in the cold, was methanol and hot water.
• the product contains higher proportions of l,4-di-cyclohexylamino-6,7-di-hydroxyethylmercaptoand l ,4-di-cyclohexylamino-6,7-di-B;y-dihydroxypropylmercaptoanthraquinone as impurities than the reaction product obtained according to (b).
• EXAMPLE 5 a 10 Parts l,4-di-cyclohexylamino--chloro-anthraquinone are dissolved in 50 parts dimethyl formamide and the solution oi oi 05 05 m I A v 3 m io io io m m 5 .5 5 io mo io w 25m 5 5 58m 5 E0 1 50$ 50 l 50 m I 12 6 m mo mo mo mo m m 6 .oflzmm HHQLWHULHHO'WI mo mo mmo w I I I I I I I I I I 1 I I I I v :OU I 1 I v I I I I I I
• reaction products B of Table I] can be obtained by the method described in Example 5 from the starting compounds A by reaction with thioglycerol.
• the shades given in the last column refer to polyamide dyeings obtained according to the dyeing instruction of Example 66.
• a printing paste is prepared from 10 parts 1,4-di-npropylamino 6-hydroxyethylmercapto-7-chloro anthraquinone (obtained according to Example 2) in finely divided form, parts Glyecin A thiodiethylene glycol, 50 parts urea, 500 parts of a 12 percent carob bean flour ether thickening, and made up with water to 1,000 parts.
• This printing paste is applied to a fabric of synthetic polyamide according to known processes by machine or screen printing, the fabric is dried, steamed in a Mather-Flatt a P paratus at 102 for 10 minutes, subsequently rinsed in the usual way andsoaped. A clear blue print of very good fastness 30 to washing, light and rubbing is obtained.
• EXAMPLE 68 a 452 Parts l,4-di-m-toluidino-6-chloro-anthraquinone are suspended at 100 in 452 parts dimethyl formamide. This suspension is admixed at 1001 10 within 20 minutes, while stirring, with a solution of 102 parts thiogl I toluidino-6 quality,
• EXAMPLE 69 a 487 Parts l,4-di-m-toluidino-5,8-dichloro-anthraquinone are stirred at 100 120 into 487 partsdimethyl formamide. To the suspension which is readily stirrable there is added at 120' 110 within 15 minutes a solution of 97.5 parts of thioglycol and 70 parts potassium hydroxide in 97.5 parts methanol, and stirring is continued at 1 for minutes.
• the mixture is diluted with 480 parts by volume of methanol, stirring is continued for 2 hours while cooling with ice, the product is filtered off with suction and the filtered material is successively washed with 1,000 parts by volume methanol and hot water. After drying, there are obtained 440 parts 1,4-di-m-toluidino-5-hydroxyethyl-mercapto-8-ch1oroanthraquinone.
• This product contains about 10 percent each of 1 ,4-di-m-toluidino-5,8-dihydroxyethyl-mercaptoanthraquinone and 1,4-di-m-toluidino-5,8-dich1oroanthraquinone as impurities.
• EXAMPLE 70 a 12.9 Parts I,4-di-anilino-5,8-dibromo-anthraquinone are dissolved in 50 parts dimethyl formamide and the solution is mixed at 90 100 with 4.65 parts thioglycol (in the form of a concentrated ethanolic solution potassium salt.) Stirring is continued at 100 105 for minutes, the mixture is cooled to 10, the precipitated dyestuff is filtered off with suction, washed with a little dimethyl formamide, subsequently with hot water, and dried. 8.2 Parts l,4-di-anilino-5,8- dihydroxyethylmercapto-anthraquinone are obtained.
• the 1,4-di-anilino-5 ,B-dibrQmo-anthraquinone can easily be obtained from 5,8-dibromoquinizarine by one of the methods described under 69 (b) (d).
• EXAMPLE 71 a 6.3 Parts 1,4-di-p-anisidino 5-chloro-anthraquinone are dissolved in parts dimethyl formamide and the solution is mixed with 2.05 parts thioglycol (on the form of a concentrated solution of the potassium salt in dimethyl formamide) at and stirred at the same temperature for 20 minutes. 15 parts of'water are then added dropwise, the product is filtered off with suction and washed with water. After-drying, there are obtained 5.05 parts l,4-di p-anisidino- 5-hydroxyethylmercapto-anthraquinone.
• EXAMPLE 72 8.5 Parts 1,4-di-m-toluidino-6,7-dichloro-anthraquinone are dissolved in 40 parts dimethyl formamide, 3.6 parts thioglycol in the form of methanolic solution of thepotassium salt are added dropwise at 100 105 in the course of 20 minutes, and stirring is continued at the same temperature for 20 minutes. The mixture is diluted with 70 parts methanol, the product is filtered off with suction, washed with methanol and hot water. 7.4 Parts l,4-di-m-toluidino-6,7-dihydroxyethylmercapto-anthraquinone are obtained.
• the 1,4-di-m-toluidino-6,7-dichloro-anthraquinone can be obtained in the following way, for example:
• reaction products B of Table 1 can be obtained by one 60 of methods described in Examples 68(11) 73(a) fro starting materials a of Table 1 by reaction with thi figures in brackets refer to the substitution anthraquinone nucleus. The shades given in refer to polyamide dyeings obtained accordin tion of Example 131.
• EXAMPLE 132 A printing paste is prepared from 10 parts l,4-di-mtoluidino6-hydroxyethylmercapto-anthraquinone (in finely divided form), 30 parts Glyecin A thiodiethylene glycol, 50 parts urea, 500 parts of a 12 percent carob bean flour ether thickening, and made up to 1,000 parts with water.
• This paste is applied to a fabric of synthetic polyamide according to known processes by machine orscreen printing, the fabric is dried and steamed in a Mather-Flatt apparatus at 102 for 10 minutes, and subsequently rinsed and soaped in the usual way. A green print of very good fastness to washing, light and rubbing is obtained.
• EXAMPLE 133 If the l ,4-di-m-toluidino-6-hydroxyethylmercaptoanthraquinone is replaced in Example 131 or 132 with the same amounts of dyestufi's obtained in Examples 69 74, then the dyestuff of Example 69(a) yields yellowish green, that of 70(a) yields bluish-green, those of 71 74(0) yield green dye- 3 5 ings or prints of good to very good fastness properties.
• R and R are selected from the group consisting of hydrogen, alkyl of one to six carbon atoms, hydroxyalkyl with one to six carbon atoms, alkoxy with one to four carbon atoms, hydroxyalkoxy with one to four carbon atoms, methoxyalkoxy with one to four carbon atoms in the alkyl radical, alkyl mercapto with one to four carbon atoms, fluoro, chloro, bromo, amino, methylamino, dimethylamino, cyclo-hexylamino, acetylamino, propionylamino, butyrylamino, acetylmethylamino, hydroxy-e
• X is an alkylene radical or an alkylene radical substituted on OH wherein alkylene means a member selected from the group C straight-chain alkylene and C branched chain alkylene;
• Y is H, Cl, Br, or a radical SX-OH; wherein the anthraquinone nucleus may contain further Cl or Br substituents wherein ii and m stand fora number from 0-3.

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Citations (1)

• 1968
  • 1968-06-29 DE DE19681768788 patent/DE1768788A1/de active Pending
• 1969
  • 1969-05-28 CH CH382770A patent/CH525269A/de not_active IP Right Cessation
  • 1969-06-20 US US835222A patent/US3666778A/en not_active Expired - Lifetime
  • 1969-06-26 GB GB1264643D patent/GB1264643A/en not_active Expired
  • 1969-06-27 FR FR6921862A patent/FR2013367B1/fr not_active Expired
  • 1969-06-27 AT AT618769A patent/AT291182B/de active
  • 1969-06-27 BE BE735322D patent/BE735322A/xx unknown
  • 1969-06-27 JP JP44050655A patent/JPS4812049B1/ja active Pending
  • 1969-06-30 NL NL6910008A patent/NL6910008A/xx unknown

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